Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Epileptic Disord ; 3(2): 57-62, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11431166

RESUMO

We investigated the electroclinical features of 12 patients with childhood absence epilepsy (CAE), presenting with typical absence seizures associated with myoclonic manifestations of the face or neck. All patients underwent repeated and prolonged split-screen video-polygraphic EEG recordings. The polygraphic recordings and clinical correlations of the absence seizures were analysed. All patients presented with multi-quotidian, typical absence seizures. During the absences, the patients could show mild, rhythmic, myoclonic jerks involving facial areas (eyebrows, nostrils, perioral region, chin) or neck muscles (sternocleidomastoideus), with the same frequency as the spike-wave complexes. Polygraphic tracings demonstrated that the myoclonias were correlated to the spike component. Clinically, all patients showed a benign course, with complete seizure control under antiepileptic treatment. In the follow-up, 7 patients withdrew from treatment without relapse. We conclude that all our patients showed an electroclinical picture consistent with CAE. The occurrence of myoclonic manifestations of the face or neck associated with the absences did not influence the benign course of their disease. The electroclinical features observed in our group of patients differentiates our cases both from epilepsy with myoclonic absences and from absences with perioral myoclonia (with Video).


Assuntos
Epilepsias Mioclônicas/fisiopatologia , Epilepsia Tipo Ausência/fisiopatologia , Criança , Pré-Escolar , Eletroencefalografia , Músculos Faciais/fisiopatologia , Feminino , Humanos , Masculino , Gravação em Vídeo
2.
Epilepsy Res ; 35(1): 29-37, 1999 May.
Artigo em Inglês | MEDLINE | ID: mdl-10232792

RESUMO

This was a prospective open comparative pilot study to assess the efficacy and tolerability of first-line vigabatrin monotherapy in childhood partial epilepsies. Two groups of patients were recruited over the same period. The vigabatrin monotherapy group comprised 40 patients (18 male, 22 female; mean age at last visit 7.5 years); the comparative carbamazepine monotherapy group comprised 40 consecutive clinic patients (22 male, 18 female; mean age at last visit 7.8 years). Seizures disappeared in 82% of vigabatrin patients and in all carbamazepine patients with idiopathic partial epilepsy, and in 50% of vigabatrin patients and 55% of carbamazepine patients with symptomatic partial epilepsy. Interictal EEG abnormalities decreased in vigabatrin patients more than in carbamazepine patients (P < 0.05). Tolerability was good in vigabatrin patients, but four out of 37 showed mild irritability by the end of the trial. Persistent sedation was observed in eight of the 40 patients receiving carbamazepine. No patient had drug therapy discontinued because of side-effects. During vigabatrin long-term monotherapy, efficacy and good clinical tolerability were maintained. These results suggest that vigabatrin may be an alternative first-line treatment for childhood partial epilepsies. Further blinded comparative randomized trials are needed.


Assuntos
Anticonvulsivantes/uso terapêutico , Epilepsias Parciais/prevenção & controle , Ácido gama-Aminobutírico/análogos & derivados , Adolescente , Anticonvulsivantes/efeitos adversos , Carbamazepina/uso terapêutico , Criança , Pré-Escolar , Eletroencefalografia/efeitos dos fármacos , Feminino , Seguimentos , Humanos , Lactente , Masculino , Projetos Piloto , Estudos Prospectivos , Vigabatrina , Ácido gama-Aminobutírico/efeitos adversos , Ácido gama-Aminobutírico/uso terapêutico
3.
Epileptic Disord ; 1(4): 217-20, 1999 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10937156

RESUMO

We report the case of a child with benign partial epilepsy with centro-temporal spikes (BECT) in whom protrusion of the tongue stopped the interictal abnormalities, and describe the polygraphic EEG recording of a seizure which terminated upon voluntary protrusion of the tongue. We mention the close link between the post-central (somatosensory) cortex and pre-central (motor) cortex, and how the primary sensory area has direct access to the motor cortex. We also examine how a tactile stimulus may provoke the inhibition of an epileptic discharge.


Assuntos
Eletroencefalografia , Epilepsia Rolândica/terapia , Hábitos Linguais , Criança , Epilepsia Rolândica/diagnóstico , Epilepsia Rolândica/genética , Epilepsia Rolândica/fisiopatologia , Potenciais Evocados/fisiologia , Seguimentos , Humanos , Masculino , Córtex Motor/fisiopatologia , Inibição Neural/fisiologia , Vias Neurais/fisiopatologia , Córtex Somatossensorial/fisiopatologia , Língua/inervação
4.
Brain Dev ; 16(4): 329-34, 1994.
Artigo em Inglês | MEDLINE | ID: mdl-7818031

RESUMO

Despite growing interest in the Landau-Kleffner syndrome there have been few reports dealing with language disorders in recent years. The authors present a clinical case of a child with Landau-Kleffner syndrome focusing particularly on the relationship between language disorders and electroencephalographic abnormalities. The authors emphasize that the language disorders primarily affect the receptive sphere and that there seems to be a relationship between abnormalities during sleep with a deterioration in verbal comprehension.


Assuntos
Eletroencefalografia , Transtornos do Desenvolvimento da Linguagem/fisiopatologia , Pré-Escolar , Feminino , Humanos , Desenvolvimento da Linguagem , Testes de Linguagem , Distúrbios da Fala/fisiopatologia , Síndrome
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...